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Publications by Michael Brauckhoff

Frequent EPAS1/HIF2 Exons 9 and 12 Mutations in Non-Familial Pheochromocytoma

Endocrine-Related Cancer
Cancer ResearchEndocrinologyOncologyMetabolismDiabetes
2014English

Germ-Line Mutations in Nonsyndromic Pheochromocytoma

New England Journal of Medicine
Medicine
2002English

Related publications

Mutational Profile and Genotype/Phenotype Correlation of Non-Familial Pheochromocytoma and Paraganglioma

Oncotarget
Oncology
2019English

Somatic NF1 Inactivation Is a Frequent Event in Sporadic Pheochromocytoma

Human Molecular Genetics
MedicineGeneticsMolecular Biology
2012English

Germline Mutations in TMEM127 Confer Susceptibility to Pheochromocytoma

Nature Genetics
Genetics
2010English

Absence of the BRCA1 Del (Exons 9–12) Mutation in Breast/Ovarian Cancer Families Outside of Mexican Hispanics

Breast Cancer Research and Treatment
Cancer ResearchOncology
2009English

Short Tandem Repeats in Human Exons: A Target for Disease Mutations

BMC Genomics
BiotechnologyGenetics
2008English

Familial Catecholamine-Secreting Tumors - Three Distinct Families With Hereditary Pheochromocytoma

2011English

PCNT Point Mutations and Familial Intracranial Aneurysms

Neurology
Neurology
2019English

GCM2 -Activating Mutations in Familial Isolated Hyperparathyroidism

American Journal of Human Genetics
Genetics
2016English

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